Electric Double-layer Capacitor Electrode Research Articles

Highly porous carbon with selective transformation of nitrogen groups boosts the capacitive performance through boric acid template assisted strategy

To address the extensive demand for energy storage, the development of unique carbon-based supercapacitors represents a viable solution. We successfully synthesize the unique boron (B), nitrogen (N)-containing porous carbon (denoted as BNPC) from reed biomass through one-step boric acid templated carbonization method, which are used as high-performance carbon electrode for electric double-layer capacitor (EDLC). By the synergistic effects of boric acid template and N-rich melamine, a well-balanced micro‐/meso-porous structure and abundant N and oxygen (O) heteroatoms within BNPC are readily obtained, exhibiting an ultrahigh specific surface area of 2619 m2·g−1. These distinctive natures endow BNPC electrode with the excellent capacitive behaviors, affording an outstanding specific capacitance of 396.8 F·g−1 at a three-electrode (3E) system with KOH electrolyte. Density functional theory (DFT) method is utilized to further clarify the interaction mechanism between K and designed graphene with various N configurations, revealing the significant roles of Pyridinc-N and Graphitic-N. The two-electrode (2E) symmetric supercapacitor assembled by BNPC electrodes in TEABF4 electrolyte demonstrates an extremely high energy density of 51.82 Wh·kg−1 at a power density of 375 W·kg−1 and great capacitance retention of 91 % after 6000 cycles. This reed-derived highly porous carbons display superior electrochemical performance, making it the ideal candidates for large capacity supercapacitors in practice.

Dynamic Effect of Overscreening on Electrochemical and Thermal Properties of EDLC Electrodes during Charging/Discharging Cycles

Overscreening was commonly observed during charging/discharging cycles of electric double layer capacitors(EDLCs). This study presented a two-dimensional continuum electrochemical thermal model with a distribution function for concentration considering overscreening to investigate how overscreening affected the dynamic formation of electric double layer (EDL) near electrodes in macroscale. The results indicated that ion distribution was co-affected by EDL formation and overscreening near the electrode. Correspondingly, layered space charge density distribution resulted in a thicker diffuse layer, whose thickness was determined by the sum of co-ion and counter-ion diameters. Additionally, the diffuse layer capacitance was proportional to the reciprocal of counter-ion diameter, while the total capacitance was proportional to a linear combination of counter-ion and the larger ion diameters. Moreover, the shift from endothermic to exothermic for the total heat generation rate was dominated by heat of mixing, and was caused by the local ion mixing due to overscreening, resulting in local entropy increase. The results of this study can be used to further investigate the effect of overscreening on ion transient transport dynamic and heat generation rates.

Microgrid-Patterned Ni Foams as Current Collectors for Ultrafast Energy Storage Devices

Current research is focused on developing active materials through surface functionalization, porosity, composites, and doping for ultrafast electric double layer capacitors (EDLCs). In this study, deviating from existing strategies focused on active materials, we designed tunable 3D microgrid-patterned (MP) surface morphologies on Ni foams used as current collectors using SUS meshes as rigid stamps during roll pressing. The surface geometries of the MP-Ni foams were controlled to standard mesh scales of 24, 40, and 60 (denoted as 24MP-Ni, 40MP-Ni, and 60MP-Ni, respectively). The three MP-Ni samples with different microgrid sizes presented different surface geometries, such as root-mean-square roughness (Rrms), skewness roughness (Rsk), and width/depth scales of the microgrid patterns. Consequently, 40MP-Ni demonstrated an optimized surface geometry with high Rrms (35.4 μm) and Rsk (−0.19) values, which facilitated deep slurry infiltration and increased its contact area with the active material. Surface optimization of the MP-Ni enabled ultrafast and reversible charge transport kinetics owing to its relaxed electron transfer resistance and robust adhesion to the active material compared with bare Ni foam. EDLC electrodes with 40MP-Ni achieved an ultrafast-rate capability (96.0 F/g at 20 A/g) and ultrafast longevity (101.9% capacity retention after 5000 cycles at 5 A/g) without specific modification of active material.

One-step generation of hollow graphitic carbon nanospheres with suitable oxygenated structures as conductive additives for water-soluble binder in highly stable supercapacitor electrodes

Although the weight ratio of electron conductive additives and the binder to porous carbons in the electrode component of electric double-layer capacitors (EDLC) is minimal, however, without them the electrochemical performances of EDLC would decay quickly. In this work, we present a one-step approach for manufacturing a unique conductive carbon material that shows highly connecting hollow structures as well as approximate oxygenated surface groups to create a synergy effect with aqueous binder and the main component, porous carbon. The as-prepared carbon nanospheres (HCNs) were generated from a typical carbon black-PC20 in air (denoted as PC20HT) at mild temperatures ranging from 400 to 700 °C for 2–4 h at a massive scale of approximate 1 kg h−1. The as-prepared PC20HT displays a high specific surface area of 657 m2 g−1 (the pristine PC20 has 112 m2 g−1) with a pore volume of 0.71 cm3 g−1, and an oxygen content of 14.10 wt%. Interestingly, a premixing of PC20HT and porous carbon is required before making the electrode pastes. The well-premixed carbon materials and a water-soluble binder-polyacrylic acid are composed into highly-stable components as EDLC electrodes in an organic electrolyte. As consequently, the PC20HT-assisted electrodes demonstrate highly stable life cycles (charge-discharge behaviors), with a retention rate 82.13 % over 50,000 cycles at a narrow voltage window of 2.5–2.7 V at 0.5 A g−1 when compared to two conventional conductive carbons, BP2000 (68.45 %) and Super P (67.46 %). Thermal annealing at 900 °C in Ar reduces the oxygen content of PC20HT to 4.25 wt% (referred to as TPC20HT), increasing the retention rate of life cycle to 88.89 % after the same cycles. TPC20HT-assisted EDLC electrodes exhibit a superior energy density of 34.76 Wh kg−1, which is higher than CB-BP2000 and Super P-assisted EDLC electrodes. The transforming of structural morphologies as well as the surface oxygenated and graphitic structures of the as-prepared HCS, PC20HT, and TPC20HT were also described before and after long-term cycling. This simple route for producing conductive carbons is applicable in an aqueous binder system for preparing EDLC electrodes with a cost-effective and environmentally friendly approach.

Mesoporous nanoplates consisting of seamless graphene frameworks

Electric double-layer capacitors (EDLCs) have attracted significant attention in the field of energy storage due to their high specific power, superior safety, and long cycle life. However, commercially available electrode materials, such as activated carbons, are still facing the challenge of low energy density. Graphene mesosponge (GMS) has shown promise as an electrode material for EDLCs due to its mesoporous structure, large specific surface area, and edge-free properties that allow operation under wide potential windows. Nevertheless, GMS materials reported so far consist of large micro-particles above 30 μm, which is unfavorable in terms of the long ion-diffusion path within the particles. In this study, a novel nanoplate GMS (np-GMS) is synthesized via a template carbonization approach, where chemical vapor deposition is performed onto a nanoplate MgO. The np-GMS exhibits a nanoplate structure with a lateral nanoplate size of approximately 1 μm and a nanoplate thickness of less than 100 nm. When employed as an electrode for EDLCs, the np-GMS shows a specific capacitance of 132 F g−1 in the potential window of −0.5 V to 1.5 V vs. Ag/AgClO4. Moreover, the np-GMS-included EDLCs demonstrate a specific energy of 59 Wh kg−1 under a voltage window of 3.5 V, which outperforms the counterpart GMS with a larger particle size and commercialized activated carbon. The introduction of np-GMS is believed to open up new possibilities for improving the performance and industrial feasibility of GMS in EDLCs.

A comprehensive study on effect of carbon nanomaterials as conductive additives in EDLCs

This study performs a comprehensive investigation to objectively analyze the effects of various carbon nanomaterials using as conductive additives (5 wt%) in activated carbon (AC) based electrodes for electrical double-layer capacitors (EDLCs). A variety of carbon nanomaterials including carbon black (CB), single-walled carbon nanotubes (SWCNT), graphene nanoplatelets (GNP), fullerenes (C60), and activated carbon nanofibers (ACNF) are considered in this work as they provide a diverse combination of intrinsic properties such as specific surface area, conductivity, micro-mesoporous structures, and geometry of nanomaterials. These additives are incorporated into freestanding carbon electrodes, and their EDLC performance in a neutral aqueous electrolyte is investigated by means of electrochemical measurements. The findings from this work provide useful insight into how the properties of various carbon nanomaterials influence EDLC performance in different aspects such as capacitive behavior, resistivity, performance at different current densities, charge propagation properties, and stability over long-term cycling. The results show that each carbon additive has its own strengths and limitations for different performance parameters considered. The unfavorable material properties of C60 cause a significant decrease in capacitance at high current density, leading to the lowest device performance incorporated with C60 as additives. While GNP and SWCNT show high crystallinity, low ID/IG ratios, the EDLCs still exhibit decreased specific capacitance and moderate energy densities due to their relatively limited specific surface area and high resistivity of the resultant composite electrodes compared to the pristine AC. The CB additives-based samples demonstrate the highest conductivity of dry electrodes and low equivalent series resistance (ESR) in EDLCs. On the other hand, a reduction in capacitance at high current densities and material degradation during long-term cycling are observed for CB samples, which could be attributed to the high dispersibility of CB causing limited interparticle voids and thus increasing diffusion resistance. In contrast, the use of ACNFs significantly reduces the diffusion resistance and improves the cyclic stability compared with CB based samples due to the advantages of larger specific surface area and superior micro-mesoporous structures of ACNFs. In particular, EDLCs with ACNFs demonstrate an increase in specific capacitance and energy density by 99 % and 76 %, respectively compared to CB based EDLCs at a current density of 20 A/g. This work elucidates the complex interplay between carbon nanomaterials using as additives and corresponding EDLC performance. These results provide important information to the community for future development of new energy conversion and storage devices.

Few-layer graphene as an ‘active’ conductive additive for flexible aqueous supercapacitor electrodes

We demonstrate that few layer graphene (FLG), formed by high-shear exfoliation into an aqueous suspension, can be successfully employed as an ‘active’ conductive additive in flexible activated carbon-based aqueous electric double layer capacitor (supercapacitor) electrodes if introduced by a novel ‘vacuum infiltration’ technique. The effectiveness of the FLG can be optimised by tailoring its size distribution and loading. It is found that best performance is achieved using FLG with the broadest size distribution and, moreover, that the larger size distribution is effective over the broadest range of loading. With optimum size distribution and loading, FLG is shown to outperform a commercial carbon black conductive additive (Timcal C65). Electrodes containing 8 wt% infiltrated FLG have an equivalent series resistance (ESR) of 1.3±0.4Ω, and a specific capacitance of 142.3±0.1 F g−1 over a voltage window of 1.2 V, compared with an ESR of 3±1Ω and a specific capacitance of 96.81±0.02 F g−1 for equivalent electrodes produced with an optimal loading of carbon black additive. As a result, the specific energy density of electric double layer capacitors (EDLCs) produced with a vacuum infused FLG additive is demonstrated to be an average of 47±3% superior to those containing carbon black measured at similar power densities. In contrast to vacuum infiltration, direct mixing of FLG suspension into the electrodes is found to be ineffective, resulting in limited improvement relative to electrodes without conductive additive, the reasons for which are discussed.

Microwaved-Assisted Synthesis of Starch-Based Biopolymer Membranes for Novel Green Electrochemical Energy Storage Devices.

The investigated starch biopolymer membrane was found to be a sustainable alternative to currently reported and used separators due to its properties, which were evaluated using physicochemical characterization. The molecular dynamics of the biomembrane were analyzed using low-field nuclear magnetic resonance (LF NMR) as well as Raman and infrared spectroscopy, which proved that the chemical composition of the obtained membrane did not degrade during microwave-assisted polymerization. Easily and cheaply prepared through microwave-assisted polymerization, the starch membrane was successfully used as a biodegradable membrane separating the positive and negative electrodes in electric double-layer capacitors (EDLCs). The obtained results for the electrochemical characterization via cyclic voltammetry (CV), galvanostatic charge with potential limitation (GCPL), and electrochemical impedance spectroscopy (EIS) show a capacitance of 30 F g-1 and a resistance of 2 Ohms; moreover, the longevity of the EDLC during electrochemical floating exceeded more than 200 h or a cyclic ability of 50,000 cycles. Furthermore, due to the flexibility of the membrane, it can be easily used in novel, flexible energy storage systems. This proves that this novel biomembrane can be a significant step toward ecologically friendly energy storage devices and could be considered a cheaper alternative to currently used materials, which cannot easily biodegrade over time in comparison to biopolymers.

Preparation of flexible and binder-free lignin-based carbon nanofiber electrode materials by electrospinning in aqueous system

Abstract Lignin, as a widely distributed, renewable and environmentally friendly source of carbon, could been utilized for carbon nanofibers to not only maximize the usage of resources, but also expand the energy-related opportunities. In this research, flexible lignin-based carbon nanofibers are prepared by electrospinning lignin nanofibers in a new green aqueous solution of lignin and polyvinyl alcohol (PVA), which is then characterized by physical and chemical characterizations. The results reveal that optimal carbonization temperature of 800 °C shows great improvements on the structural properties of lignin-based carbon nanofibers, which can be applied as binder-free electric double layer capacitor (EDLC) electrodes with good flexibility. The 2032 type button battery has a superior electrochemical performance with a large specific capacitance of 217.2 F g−1 at a 0.2 A g−1 current density, and remarkable cyclic stability of 94.9 % capacitance retention even after 10,000 charge and discharge cycles, due to the abundance of mesoporous volume and large microporous surface area of lignin-based carbon nanofiber electrodes carbonized in 800 °C.

An artificial neural network model for capacitance prediction of porous carbon-based supercapacitor electrodes

Among energy storage devices, the last decades have witnessed the rapid spread of usage of carbon-based electrodes for electric double-layer capacitors (EDLCs) due to their large surface area, low cost, and high porosity. It is crucial to develop an accurate and efficient forecasting model for electrochemical performance to reduce the time needed for making suitable designs and choosing testing electrode materials. As a result, the use of machine learning (ML) approaches in creating a predicting model for the capacitance of carbon-based supercapacitors looks critical and provides the electrode characteristics' relative relevance. Data extracted from nearly a hundred published experimental research papers to select supercapacitors with certain electrode morphologies such as mesoporous, nanoporous, microporous, and hierarchical porous carbon electrode. The data was examined using machine learning techniques to predict the supercapacitor's specific capacitance (F/g). Electrode material structural qualities and various physicochemical test features such as electrolyte material, pore volume, and specific surface area. Electrochemical test features acquired via electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD) test investigations for the same purpose include: cell configuration, current density, applied potential window, charge-transfer resistance (RCT), and equivalent series resistance (ESR) were used as input features to predict the corresponding capacitance performance. In the present study, Lasso, Support Vector Machine Regression (SVMR), and Artificial Neural Networks (ANN) with different structures were examined to predict the capacitance of the supercapacitor. The exhibition of the ML models measured concerning the root mean square error (RMSE), the correlation between expected yield and yield provided by the system. The developed ANN model with RMSE, MAE, and R values of 30.82, 46.5624 and 0.89537, respectively, provides outcomes for the prediction that are highly accurate compared to other models created for this purpose. According to the analysis of the input features done using the SHAP (SHapley Additive exPlanations) framework, the specific surface area had the biggest impact on the ANN model.

Preparation and Characterization of Asphalt Pitch-Derived Activated Carbons with Enhanced Electrochemical Performance as EDLC Electrode Materials

This study used a physical activation method to prepare asphalt-pitch-derived activated carbon (Pitch AC) for an electric double-layer capacitor (EDLC) electrode. X-ray diffraction analysis and Raman spectroscopy were used to estimate the change in the crystal structure of Pitch AC with activation time. In addition, the textural properties of Pitch AC were studied by Brunauer-Emmett-Teller (BET), Dubinin-Radushkevich (DR) and non-localized density functional theory (NLDFT) equations with N2/77K isotherm adsorption-desorption curves. The electrochemical performance of the Pitch AC was analyzed using a coin-type EDLC with 1 M SBPBF4/PC via galvanostatic charge/discharge, cyclic voltammetry and electrochemical impedance spectroscopy. The specific surface area and total pore volume were 990–2040 m2/g and 0.42–1.51 cm3/g, respectively. The pore characteristics of the Pitch AC varied according to the activation time and changed from a microporous structure to a micro-mesoporous structure as the activation time increased. The electrochemical performance analysis also found that the specific capacity was increased from 43.6 F/g to 84.5 F/g at 0.1 A/g as activation time increased. In particular, Pitch AC-9 exhibited the best electrochemical performance (rectangular CV curve, reversible GCD, lowest ion charge transfer resistance and Warburg impedance). In addition, Pitch AC-9 was confirmed to have a specific capacitance similar to commercial activated carbon for EDLC (YP-50F). Therefore, it was considered that Pitch AC could replace commercial activated carbon for EDLC because it has excellent pore characteristics and electrochemical performance despite being manufactured through a very low-cost precursor and a simple process (physical activation method).

Fast Ion Transfer Associated with Dehydration and Modulation of Hydration Structure in Electric Double-Layer Capacitors Using Molecular Dynamics Simulations and Experiments

Carbon materials, such as graphite and activated carbon, have been widely used as electrodes in batteries and electric double-layer capacitors (EDLCs). Graphene, which has an extremely thin sheet-like structure, is considered as a fundamental carbon material. However, it was less investigated as an electrode material than graphite and activated carbons. This is because graphene is a relatively new material and is difficult to handle. However, using graphene electrodes can enhance the performance of nanodevices. Here, the performance of EDLCs based on single-layer and bilayer graphene electrodes in LiCl, NaCl, and KCl aqueous electrolyte solutions was evaluated using cyclic voltammetry, and the charging mechanism was evaluated using molecular dynamics simulations. KCl aqueous solution provided the highest capacitance compared to LiCl and NaCl aqueous solutions in the case of single-layer graphene electrodes. In contrast, the dependence of the capacitance on the ion species was hardly observed in the case of bilayer graphene. This indicates that Li and Na ions also contributed to the capacitances. The high EDLC performance can be attributed to the fast ion transfer promoted by the dehydration and modification of the second hydration shell on the bilayer graphene because of the relatively strong interaction of ions with the bilayer graphene.

Simple synthesis of nitrogen-doped zeolite-templated carbon and its use in electric double-layer capacitors

Nitrogen-doped zeolite-templated carbon (N-doped ZTC) is synthesized using NaY zeolite as a template and with acrylonitrile (AN) and propylene as the respective nitrogen and carbon sources. AN is directly mixed with the dried zeolite for adsorption and the mixture is heated to synthesize polyacrylonitrile (PAN) inside the zeolite micropores. Each AN adsorption and polymerization step require only 1 h and both steps were performed in a single container. The resulting zeolite/PAN composite was then subjected to chemical vapor deposition using propylene to fill the zeolite pores with carbon. Subsequently, heat treatment was used for carbonization and the zeolite was removed with hydrofluoric acid. The N-doped ZTC has three-dimensionally ordered and interconnected micropores with a uniform pore size of 1.2 nm, inheriting the structural regularity of the zeolite. The optimum volume of AN is determined to be the same as the total pore volume of the zeolite, which accounts for the high surface area of 3680 m2 g−1 and high structural regularity with a N/C molar ratio of 0.015. The performance of the N-doped ZTC as an electric double-layer capacitor electrode was evaluated using an organic electrolyte and showed a superior performance to undoped ZTC and maintained a high capacitance retention up to 2 A g−1.

Porosity development of templated porous carbons dried by vacuum as carbon electrodes for electric double-layer capacitors

Resorcinol and formaldehyde (RF) resin serves as the carbon precursor for porous carbons and carbon/carbon composites possessing a high specific surface area (SSA). This work presents the porosity improvement by the elimination of cotton fibers (CF) from CF/RF composite hydrogels subsequently exchanged by tertiary butyl alcohol (TBA), dried by vacuum, and carbonized. This route contributes the templated porous carbons (TPC) with an asymmetric structure comprising micropores, mesopores, and macropores. At 0.25 of the CF/RF weight ratio, TPC dried by vacuum apparatus has SSA of 2,102 m2 g−1, whereas TPC dried by evaporation only offers SSA of 663 m2 g−1. Using the vacuum acts as pseudo-freeze drying during TBA removal, forming sponge-like carbon and allowing ultra-high SSA. The electrochemical properties of vacuumed TPCs were analyzed, showing that TPC at 0.25 of the CF/RF weight ratio possessed 626 F g−1 more than TPC at 0.00 of the CF/RF weight ratio which had 392 F g−1 at 200 mA g−1.

Utilization of starch and cellulose toward facile synthesis of high surface area zeolite-templated carbon

• Starch and cellulose are examined to synthesize zeolite-templated carbons (ZTCs). • Gravimetric surface area is maximized to 3760 m 2 g −1 by using starch. • Volumetric surface area is maximized to 790 m 2 g −1 by using cellulose. • EDLC performances of the ZTCs are evaluated using an organic electrolyte. • The present method does not use liquid-phase adsorption or any organic solvents. Starch and cellulose are examined to synthesize high surface area zeolite-templated carbons (ZTCs). In this method, starch or cellulose is mixed with undried NaY zeolite as a template, and the mixture is subject to chemical vapor deposition (CVD) using propylene and subsequent heat treatment, followed by zeolite removal with HF. For maximizing the structural regularity and surface area of ZTC, a necessary amount of starch is only equal to the total pore volume of the zeolite ( i.e. , 0.5 g per 1 g of the zeolite). Upon heating, starch is decomposed into oligosaccharides and the oligosaccharides are adsorbed inside the micropores of the zeolite before the CVD. The adsorbed oligosaccharides are pyrolyzed into nanographenes, and the nanographenes are extended and interconnected together to form the three-dimensional ZTC framework inside the zeolite pores during the CVD. The resulting gravimetric and volumetric surface areas are 3760 m 2 g −1 and 630 m 2 cm −3 , respectively. Meanwhile, cellulose is not readily decomposed into oligosaccharides, and a necessary amount of cellulose is 1.4 times larger than that that of starch to maximize the high structural regularity, yielding the gravimetric and volumetric surface areas of 3330 m 2 g −1 and 670 m 2 cm −3 , respectively. A decrease in the gravimetric surface area is explained by the formation of cellulose-derived amorphous carbons on the surface of ZTC particles. However, the difference in their volumetric surface areas is negligible because the amorphous carbons are so small that they do not expand the volume of the densified ZTC. Consequently, the ZTC prepared using cellulose shows high volumetric capacitance and high capacitance retention even at 10 A g −1 as an electric double-layer capacitor electrode, due to the existence of amorphous carbons that enhance the electrical conductivity of the electrode.

Hierarchical porous carbon foam electrodes fabricated from waste polyurethane elastomer template for electric double-layer capacitors

Plastic waste has become a major global environmental concern. The utilization of solid waste-derived porous carbon for energy storage has received widespread attention in recent times. Herein, we report the comparison of electrochemical performance of porous carbon foams (CFs) produced from waste polyurethane (PU) elastomer templates via two different activation pathways. Electric double-layer capacitors (EDLCs) fabricated from the carbon foam exhibited a gravimetric capacitance of 74.4 F/g at 0.1 A/g. High packing density due to the presence of carbon spheres in the hierarchical structure offered excellent volumetric capacitance of 134.7 F/cm3 at 0.1 A/g. Besides, the CF-based EDLCs exhibited Coulombic efficiency close to 100% and showed stable cyclic performance for 5000 charge–discharge cycles with good capacitance retention of 97.7% at 3 A/g. Low equivalent series resistance (1.05 Ω) and charge transfer resistance (0.23 Ω) due to the extensive presence of hydroxyl functional groups contributed to attaining high power (48.89 kW/kg). Based on the preferred properties such as high specific surface area, hierarchical pore structure, surface functionalities, low metallic impurities, high conductivity and desirable capacitive behaviour, the CF prepared from waste PU elastomers have shown potential to be adopted as electrodes in EDLCs.

Characteristics of graphite oxide membranes with different thickness by low temperature thermal reduction for aqueous EDLC electrodes and hot activation phenomenon

Reduced graphite oxide membrane (RGOM) with different thickness were prepared and used as electric double layer capacitor (EDLC) electrodes with aqueous electrolyte. According to quantum and molecular dynamic simulations, it was difficult for K+ and OH− to diffuse into graphene sheets due to dense structure, which made the RGOM electrodes show poor EDLC behaviors. Electrochemical tests showed that controlling the thickness of electrodes and modifying the dense structure could improve the specific capacitance of EDLC. Further studies indicated that during galvanostatic charge/discharge processes, if the EDLC were heated at 70 °C for one cycle and then cooled down to room temperature, the specific capacitance could be increased further. Additionally, according to 10,000 times cycling tests at 5000 mA g−1, the improved capacitance could be maintained for long time (154–167 F g−1 during test process), indicating that the hot activation could make RGOM electrodes obtain good and stable EDLC performances.

Comparison of Pore Structures of Cellulose-Based Activated Carbon Fibers and Their Applications for Electrode Materials.

This study presents the first investigation of cellulose-based activated carbon fibers (RACFs) prepared as electrode materials for the electric double-layer capacitor (EDLC) in lieu of activated carbon, to determine its efficacy as a low-cost, environmentally friendly enhancement alternative to nanocarbon materials. The RACFs were prepared by steam activation and their textural properties were studied by Brunauer–Emmett–Teller and non-localized density functional theory equations with N2/77K adsorption isotherms. The crystallite structure of the RACFs was observed by X-ray diffraction. The RACFs were applied as an electrode material for an EDLC and compared with commercial activated carbon (YP-50F). The electrochemical performance of the EDLC was analyzed using galvanostatic charge/discharge curves, cyclic voltammetry, and electrochemical impedance spectroscopy. The results show that the texture properties of the activated carbon fibers were influenced by the activation time. Crucially, the specific surface area, total pore volume, and mesopore volume ratio of the RACF with a 70-min activation time (RACF-70) were 2150 m2/g, 1.03 cm3/g and 31.1%, respectively. Further, electrochemical performance analysis found that the specific capacitance of RACF-70 increased from 82.6 to 103.6 F/g (at 2 mA/cm2). The overall high specific capacitance and low resistance of the RACFs were probably influenced by the pore structure that developed outstanding impedance properties. The results of this work demonstrate that RACFs have promising application value as performance enhancing EDLC electrode materials.

Vertically aligned graphene prepared by the electrochemical anodization of graphite foil for supercapacitor electrodes

Vertically aligned graphene (VAG) improves the specific capacitance of electric double layer capacitor (EDLC) electrodes, because VAGs increase the specific surface area of electrode and promote ion diffusion. Herein, we demonstrate a facile approach for preparing the VAGs with outstanding areal specific capacitance by electrochemical anodization of graphite foil (GF). As the anodizing time increases, the graphite layers in the anodized GF (AGF) electrodes expand due to ion intercalation and bubbles. Each graphite layer is vertically aligned, resulting in the formation of VAG sheets on the GF surface. The AGF electrode exhibits an excellent specific areal capacitance of 2.79 Fcm−2 at a current density of 2 mAcm−2, which is higher than that of the GF electrode by a factor of 17.43. The EDLC device using AGF electrodes exhibits an outstanding specific areal capacitance of 1.43 Fcm−2 at a current density of 2 mAcm−2 and a favorable cycling stability retaining 90% of its initial capacitance after 2000 cycles at a current density of 20 mAcm−2. This AGF electrode fabrication method is simple, cost-effective, and eco-friendly. We believe that the fabrication of AGF electrodes may be a significant contribution to the development of high-performance supercapacitors as well as the eco-friendly energy industry.

A review on the development of a porous carbon-based as modeling materials for electric double layer capacitors

Carbon electrodes are a key factor for electric double layer capacitors (EDLCs). Carbon gels have high porosity with a controllable pore structure by changing synthesis conditions and modifying preparation processing to improve the electrochemical performance of EDLCs. This review summarizes the preparation of carbon gels and their derivatives, the criteria to synthesize high surface area in each process, the development by some carbon forms, and EDLC applications. Porous carbons are also prepared as model materials by concentrating on how pore structure increases electrochemical capacitance, such as electronic and ion resistance, the tortuosity of pore channel, suitable micropore and mesopore sizes, and mesopore size distribution. This review emphasizes the significance of pore structures as the key factor to allow for the design of suitable pore structures that are suitable as the carbon electrode for EDLCs.